Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job DescriptionAnalysis Standards Associate - Statistician III ConsultantCorrect Location- TITUSVILLE, NJ (System Error)SummaryThe Analysis Standards Associate provides operational expertise in developing and managing analysis standards for clinical research.The role of the Analysis Standards Associate is to work with business stakeholders to align standards with business needs, provide standards guidance to content subject matter experts (SMEs) developing or updating standards content, review and QC standard SAS code, and support and align with relevant industry standards.Key ResponsibilitiesWork with business stakeholders to define, review, QC, and maintain standard statistical requirements aligned with business needs and industry standardsReview and QC ADaM dataset and result metadata aligned with documented statistical requirements and industry standardsReview and QC SAS programs and macros that create standard ADaM datasets and tables, figures, and listings based on documented statistical requirementsDevelop, review and maintain documentation describing standards and related processes and business rulesProvide support for business stakeholders implementing standards including communications, training, Q&A, compliance and usage metricsAssist with coordination of standards development projectsAssist with management, assessment, and execution of change requestsAssist with maintenance of the standards repositoryQualifications and CompetenciesBS/BA degree in statistics (preferred), computer science, mathematics, or other scientific field5+ years as a statistician or similar position with clinical research analysis and reporting responsibility in a biopharma or CRO environmentBasic knowledge in SAS programming with experience developing programs for QC/validation purposesSolid understanding of the principles and practices of clinical research analysis and reporting with Statistical Analysis Plan development experienceBasic knowledge of relevant industry standards (ie, ADaM and SDTM with focus on ADaM specifications experience ) and solid knowledge of regulatory requirementsStrong English verbal and written communication skillsExperience working in a virtual team environment with good collaboration, organizational, communication, and problem-solving skillsAbility to prioritize tasks and work effectively in a fast-paced multi-project environmentQualificationsBS/BA degree in statistics (preferred), computer science, mathematics, or other scientific fieldAdditional InformationRegards,Akriti GuptaAssociate Recruiter (Clinical / Scientific Division)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: 973.967.3409 | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: ResearchExperience level: Mid-Senior LevelIndustry: Pharmaceuticals
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